| Tag | Content |
|---|
EnhancerAtlas ID | HS098-59751 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chrX:69699120-69700570 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Hnf4a | MA0114.3 | chrX:69699796-69699812 | CAGGTCAAAGTACAAA | + | 6.13 | | NFIA | MA0670.1 | chrX:69699916-69699926 | GGTGCCAAGT | + | 6.02 | | ZIC1 | MA0696.1 | chrX:69700354-69700368 | TACCTCCCGCTGTG | + | 6.19 | | ZIC3 | MA0697.1 | chrX:69700354-69700369 | TACCTCCCGCTGTGA | + | 6.36 | | ZNF263 | MA0528.1 | chrX:69699674-69699695 | GGAAGAGGGAGGGGGTGGAGG | + | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGCCCTTCAG AGCACTAGCC CTTGTGCTGG ACGAGGAGAG CTCCATGCCA ACCCAGCCCT 60
TCTTATTTAA CTAGTGGGCT AGGGAGTATG TACTCCCAGT TCTAAAATAA CGCTTCTCAC 120
TGTATGCTTA GGTTGTGTAT TTTATGGTCA GTGTCTCCTC CCTTTTGTGA GCTGGCTTCT 180
TCCTTTTAGC TCATGAATGA CTCAGTATGG GAAAATTTCA GTTTGCTCTA ATTGTAAAAG 240
ACTGTTGGGT GATTGTTGCT AGTCAGCATT CAAATATCAG TCAAATGTTC AAAGTACTTT 300
GCTTGCAATC TGTGCTTTGA GGGGAAACTT GCCACCCCCC CATCCCCTTC CATGTATGCA 360
TAATAGACAT CAGGATTTGT ATCTGAGCAT AGCAACTATC GCAGTGTTCT GGTACAGGAT 420
CTCTTTTAAG AGACCAAAGA ACTGACAGGT TGCTGCATTC TGGATGTTTT ATTGTGATTC 480
CATTCCCCCC TCACCACCCG CTGCACTGGT CTGCTGTATC TATGAATCAT GGGATGTATA 540
GTGTATGTGC CCTAGGAAGA GGGAGGGGGT GGAGGGAACA GATAGGTAGC ATGGAGTATA 600
TTGCTGCTGA AAGCTATTCC AAGATATTTC CAAGGTTGAG CTTCTCTGAC CCTTGAGGCA 660
TAGCTTAATA CTTTGTCAGG TCAAAGTACA AATCTCCTGG GGAGTTGGAG TGCCAAGTGA 720
ATACTGTGGA CTCCTCATAG AATTAGGGAT AGCTTCCTTC TTCCTGCTTT GGCTTCTTGG 780
CAAAACTCCA AAATCTGGTG CCAAGTACAT TGTATCCTCC AAGGTTAAAG CCCTTAGAGA 840
AAGGTGGTGG GGATTACTCT CCTGAGCCAG AAGTTGCTAC AGTATTGTGT TTAATGCTTA 900
GGTGTGGGGT CATATCAAAC TCTTGGGCTG AACTTTTTCT AGTGGCCTCT GATACCTGGC 960
TGGGAAGTTG CACTTGCTAG TTGCTTGGCA ACGTGACAAC TGCTCTGTCC TTGGGGTGTG 1020
AGAGGACAAT AGTGAAGGGA TGTCAACGCT AATTGCAGTT TTTCTCATGG TGCTTGCTTT 1080
TCTTTTTCCC CAGTTGGTGG TCCCTGACTC TACCGCAGGG AGTGGAGCTA AAGGAGCCCA 1140
TCTCTGAGCC TGAAGCCCAC TAGAACCCTT CACAATCTTT CCTAATGTGA ACCCTCAACT 1200
CCACCCCTTG TGTGTTGAAA GCATGTGCTA TGCTTACCTC CCGCTGTGAA GGGAGAATGG 1260
TAGGAAGGCG GGACTAGTCA CTGGTCATTT TTCCAATTCC CCGGAAAGGA AAGTTTTGTT 1320
TTCTGTCACT AAAGCCCTTG CTCCCAGTCT GCAGCCTGGA TACTGGGGTG CTGATGGGTG 1380
AAATCAGAAA TGCACTGTCG ACCCCCCAAA ATAGGTAATG GTTATATGAC TTGGTCAGGA 1440
TTGTTCCGTT 1450
|
| |
|
|
|
